Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11434755 11 18045473 upstream gene variant -/A delins 0.41 1
rs34729281
SUGP2
19 19009572 intron variant -/G delins 2
rs562306828 20 45928576 non coding transcript exon variant -/G;GAG;GAGAG ins 1
rs151105710
STAG1
3 136406836 intron variant -/GAATTAAA delins 0.16 1
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 4
rs34696509
UVRAG
11 75841535 intron variant A/-;AA delins 0.18 1
rs34879232
SARM1 ; SLC46A1
17 28395021 3 prime UTR variant A/-;AA;AAA delins 1
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 4
rs3858076
ABCA1
9 104893841 intron variant A/C snv 0.20 3
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs4805881
PEPD
19 33405526 intron variant A/C snv 0.69 3
rs6726798
VIL1
2 218436132 intron variant A/C snv 0.94 3
rs7000460
LPL
8 19946291 intron variant A/C snv 7.9E-02 3
rs11078917 17 39590106 intergenic variant A/C snv 0.56 2
rs146524044
MYO5B
18 50057046 intron variant A/C snv 1.0E-03 2
rs353616
CD44
11 35155029 intron variant A/C snv 1.9E-02 2
rs643830
NCAM1
11 113235826 intron variant A/C snv 1.5E-02 2
rs6810819
NOCT
4 139015171 upstream gene variant A/C snv 3.4E-02 2
rs7222232
GAS7
17 10033485 intron variant A/C snv 1.3E-02 2
rs7519429
DNM3 ; PIGC
1 172380106 intron variant A/C snv 0.29 2
rs7849420
MIR31HG
9 21499625 intron variant A/C snv 0.65 2